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Epidemic retinitis - Factors associated with poor visual outcomes

PURPOSE: To identify factors other than macular edema and retinitis location responsible for poor visual outcomes in epidemic retinitis (ER). METHODS: A retrospective, observational, comparative study. Eyes with corrected distant visual acuity (CDVA) 20/200 or worse at resolution formed Group A. Eye...

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Autores principales: Kawali, Ankush, Sanjay, Srinivasan, Mahendradas, Padmamalini, Mohan, Ashwin, Shetty, Bhujang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114578/
https://www.ncbi.nlm.nih.gov/pubmed/35225539
http://dx.doi.org/10.4103/ijo.IJO_1153_21
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author Kawali, Ankush
Sanjay, Srinivasan
Mahendradas, Padmamalini
Mohan, Ashwin
Shetty, Bhujang
author_facet Kawali, Ankush
Sanjay, Srinivasan
Mahendradas, Padmamalini
Mohan, Ashwin
Shetty, Bhujang
author_sort Kawali, Ankush
collection PubMed
description PURPOSE: To identify factors other than macular edema and retinitis location responsible for poor visual outcomes in epidemic retinitis (ER). METHODS: A retrospective, observational, comparative study. Eyes with corrected distant visual acuity (CDVA) 20/200 or worse at resolution formed Group A. Eyes with central macular thickness (CMT) 600 μm or worse and retinitis within 1500 μm to foveal center at the presentation, but improved to CDVA 20/200 or better at the resolution formed Group B. The patient’s history, clinical presentation, imaging, and treatment outcomes were studied and the factors responsible for the final visual outcomes were compared in both groups. RESULTS: Groups A and B included 25 eyes each. The mean CDVA at the presentation was 20/400 (range: 20/125–20000) and 20/320 (range: 20/80–20000), and mean CMT at the presentation was 948.5 μm (range: 520–1553) and 912.2 μm (range: 615–1250) in Groups A and B, respectively. All eyes except 1 (Group A) had retinitis lesions within 1500 μm of foveal center. The mean CDVA at the resolution was 20/400 (range: 20/200–20/20000) and 20/40 (range: 20/20–20/80) in Groups A and B, respectively. Older age, male gender, diabetic status, delayed presentation, poor presenting CDVA, bilaterality, presence of keratic precipitates, disk pallor, retinal thinning, and subfoveal deposits had a statistically significant association, whereas the absence of skin rash, ellipsoid zone loss, negative WIDAL, Weil-Felix test, and delayed doxycycline therapy or use of steroids without doxycycline had a statistically insignificant association with poor visual outcomes. CONCLUSION: Apart from presenting CMT and location of retinitis, multiple demographic, clinical, and imaging factors can be implicated for poor visual outcomes.
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spelling pubmed-91145782022-05-19 Epidemic retinitis - Factors associated with poor visual outcomes Kawali, Ankush Sanjay, Srinivasan Mahendradas, Padmamalini Mohan, Ashwin Shetty, Bhujang Indian J Ophthalmol Special Focus, Retina, Original Article PURPOSE: To identify factors other than macular edema and retinitis location responsible for poor visual outcomes in epidemic retinitis (ER). METHODS: A retrospective, observational, comparative study. Eyes with corrected distant visual acuity (CDVA) 20/200 or worse at resolution formed Group A. Eyes with central macular thickness (CMT) 600 μm or worse and retinitis within 1500 μm to foveal center at the presentation, but improved to CDVA 20/200 or better at the resolution formed Group B. The patient’s history, clinical presentation, imaging, and treatment outcomes were studied and the factors responsible for the final visual outcomes were compared in both groups. RESULTS: Groups A and B included 25 eyes each. The mean CDVA at the presentation was 20/400 (range: 20/125–20000) and 20/320 (range: 20/80–20000), and mean CMT at the presentation was 948.5 μm (range: 520–1553) and 912.2 μm (range: 615–1250) in Groups A and B, respectively. All eyes except 1 (Group A) had retinitis lesions within 1500 μm of foveal center. The mean CDVA at the resolution was 20/400 (range: 20/200–20/20000) and 20/40 (range: 20/20–20/80) in Groups A and B, respectively. Older age, male gender, diabetic status, delayed presentation, poor presenting CDVA, bilaterality, presence of keratic precipitates, disk pallor, retinal thinning, and subfoveal deposits had a statistically significant association, whereas the absence of skin rash, ellipsoid zone loss, negative WIDAL, Weil-Felix test, and delayed doxycycline therapy or use of steroids without doxycycline had a statistically insignificant association with poor visual outcomes. CONCLUSION: Apart from presenting CMT and location of retinitis, multiple demographic, clinical, and imaging factors can be implicated for poor visual outcomes. Wolters Kluwer - Medknow 2022-03 2022-02-25 /pmc/articles/PMC9114578/ /pubmed/35225539 http://dx.doi.org/10.4103/ijo.IJO_1153_21 Text en Copyright: © 2022 Indian Journal of Ophthalmology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Special Focus, Retina, Original Article
Kawali, Ankush
Sanjay, Srinivasan
Mahendradas, Padmamalini
Mohan, Ashwin
Shetty, Bhujang
Epidemic retinitis - Factors associated with poor visual outcomes
title Epidemic retinitis - Factors associated with poor visual outcomes
title_full Epidemic retinitis - Factors associated with poor visual outcomes
title_fullStr Epidemic retinitis - Factors associated with poor visual outcomes
title_full_unstemmed Epidemic retinitis - Factors associated with poor visual outcomes
title_short Epidemic retinitis - Factors associated with poor visual outcomes
title_sort epidemic retinitis - factors associated with poor visual outcomes
topic Special Focus, Retina, Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114578/
https://www.ncbi.nlm.nih.gov/pubmed/35225539
http://dx.doi.org/10.4103/ijo.IJO_1153_21
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